Renaissance Pharmaceutical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Renaissance Pharmaceutical, Inc. - FDA 510(k) Cleared Devices
4
Total
1
Cleared
0
Denied
Renaissance Pharmaceutical, Inc. has 1 FDA 510(k) cleared medical devices. Based in Dana Point, US.
Historical record: 1 cleared submissions from 1994 to 1996. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Renaissance Pharmaceutical, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Renaissance Pharmaceutical, Inc.
4 devices
Cleared
Jul 15, 1996
WOUND HYDROGEL AND/OR STERILE WOUND HYDROGEL
General & Plastic Surgery
101d
Cleared
Jul 15, 1996
WOUND HYDROGEL & STERILE WOUND HYDROGEL
General & Plastic Surgery
73d
Cleared
Oct 16, 1995
WOUND HYDROGEL AND/OR STERILE WOUND HYDROGEL
General & Plastic Surgery
27d
Cleared
Jun 10, 1994
STERILE WOUND HYDROGEL DRESSING
General & Plastic Surgery
81d